T2T-YAO: a Telomere-to-telomere Assembled Diploid Reference Genome for Han Chinese

Author:

He Yukun,Chu Yanan,Guo Shuming,Hu Jiang,Li Ran,Zheng Yali,Ma Xinqian,Du Zhenglin,Zhao Lili,Yu Wenyi,Xue Jianbo,Bian Wenjie,Yang Feifei,Chen Xi,Zhang Pingan,Wu Rihan,Ma Yifan,Shao Changjun,Chen Jing,Wang Jian,Li Jiwei,Wu Jing,Hu Xiaoyi,Long Qiuyue,Jiang Mingzheng,Ye Hongli,Song Shixu,Li Guangyao,We Yue,Xu Yu,Ma Yanliang,Chen Yanwen,Wang Keqiang,Bao Jing,Xi Wen,Wang Fang,Ni Wentao,Zhang Moqin,Yu Yan,Li Shengnan,Kang Yu,Gao Zhancheng

Abstract

AbstractSince its initial release in 2001, the human reference genome has been continuously improved in both continuity and accuracy, and the recently-released telomere-to-telomere version—T2T-CHM13—reaches its top quality after 20 years of effort. However, T2T-CHM13 does not represent an authentic diploid human genome, but rather one derived from a simplified, nearly homozygous genome of a hydatidiform mole cell line. To address this limitation and provide an alternative pertinent to the Chinese population, the largest ethnic group in the world, we have assembled a complete diploid human genome of a male Han Chinese, T2T-YAO, which includes telomere-to-telomere assemblies for all the 22+X+M and 22+Y chromosomes in his two haploids inherited separately from his parents. Both haplotypes contain no artificial sequences or model nucleotides and possess a high quality comparable to CHM13, with fewer than one error per ∼14 Mb. Derived from the individual who lives in the aboriginal region of Han Chinese, T2T-YAO shows clear ancestry and potential genetic continuity from the ancient ancestors of the Han population. Each haplotype of T2T-YAO possesses ∼340 Mb exclusive sequences and ∼3100 unique genes as compared to CHM13, and their genome sequences show greater genetic distance to CHM13 than to each other in terms of nucleotide polymorphism and structural variations. The construction of T2T-YAO would serve as a high-quality diploid reference that enables precise delineation of genomic variations in a haplotype-sensitive manner, which could advance our understandings in human evolution, hereditability of diseases and phenotypes, especially within the context of the unique variations of the Chinese population.

Publisher

Cold Spring Harbor Laboratory

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